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Micro Hole for Trapping Flowing Cell

机译:捕获流动池的微孔

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摘要

Micro holes have been designed to trap a biological cell, which flows through a micro channel in vitro. Several micro traps of a half cylindrical hole of 0.002 mm depth (0.02 mm diameter) have been fabricated on the surface of the polydimethylsiloxane (PDMS) disk with the photolithography technique. A rectangular flow channel (0.1 mm depth × 1 mm width × 20 mm length) has been constructed with a silicone film of 0.1 mm thick, which has been sandwiched by two transparent PDMS disks. Two types of biological cells were used in the test alternatively: C2C12 (mouse myoblast cell line originated with cross-striated muscle of C3H mouse), or MC3T3-E1 (mouse osteogenic cell line). A constant flow (2.8 ×10~(-10) m~3/s or 8.3 ×10 m~3/s) of a suspension of cells was introduced with a syringe pump. The behavior of cells moving over the micro holes was observed with an inverted phase contrast microscope. The results show that the cell is trapped with the micro hole under the wall shear rate less than 100 s~(-1) for several seconds.
机译:设计了微孔以捕获生物细胞,该生物细胞在体外流过微通道。使用光刻技术,在聚二甲基硅氧烷(PDMS)盘的表面上制造了几个0.002毫米深(直径0.02毫米直径)的半圆柱形孔的微阱。构造了一个矩形流动通道(深度0.1毫米×宽度1毫米×长度20毫米),厚度为0.1毫米的硅胶膜被两个透明的PDMS圆盘夹在中间。替代地,在测试中使用了两种类型的生物细胞:C2C12(源自C3H小鼠的横纹肌的小鼠成肌细胞系)或MC3T3-E1(小鼠成骨细胞系)。用注射泵引入恒定流量(2.8×10〜(-10)m〜3 / s或8.3×10m〜3 / s)的细胞悬浮液。用反相显微镜观察细胞在微孔上移动的行为。结果表明,在小于100 s〜(-1)的壁剪切速率下,细胞被微孔捕获了几秒钟。

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